Warning letters, 483s, Recalls, Import Alerts, Audit observations
GMP compliance at PPL sites. Ensure implementation/remediation of the Quality systems, procedures and practices at
A role holder to Prepare batch documents (MMaRs and MPaRs) for new launch, site transfer,
Responsible for operation supports of Manufacturing Execution Systems (MES) and Document Management Systems (DMS) for
Support Managers with compliance activities for Third Party Organizations and Customer Operations. Responsible for executing
Responsible to summarize and review stability data to ensuring that Apotex commercial products’ shelf lives
To Manage the entire qualification and validation activities in the site specifically related to equipment/utility
Manage research and development quality assurance division, Responsible for Quality Systems of Development Services and
GLP Document Control, Study Protocols Issuance and Reconciliation, Clinical sample management
To ensure regulatory compliance of IT and electronic systems for Piramal critical care sites and
